Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
148293017 | Oromandibular-limb hypogenesis spectrum | en | Synonym | Active | Case insensitive | SNOMED CT core |
148294011 | Hypoglossia-hypodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
148299018 | Facial-limb disruptive spectrum | en | Synonym | Active | Case insensitive | SNOMED CT core |
832339019 | Oromandibular-limb hypogenesis spectrum (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3323616016 | A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Glossopalatine ankylosis | Is a | True | Oromandibular-limb hypogenesis spectrum | Inferred relationship | Some | |
Charlie M syndrome | Is a | True | Oromandibular-limb hypogenesis spectrum | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set